(4,4-Dimethoxybutyl)(methyl)amine → 2-(5-chloro-1-(2-(3,3-dimethylcyclopentyl)ethyl)-1H-indol-3-yl)-N-methylethanamine
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]([CH2:10][CH2:11][CH:12]2[CH2:16][CH2:15][C:14]([CH3:18])([CH3:17])[CH2:13]2)N)=[CH:4][CH:3]=1.CO[CH:21](OC)[CH2:22][CH2:23][CH2:24][NH:25][CH3:26]>>[Cl:1][C:2]1[CH:7]=[C:6]2[C:5](=[CH:4][CH:3]=1)[N:8]([CH2:10][CH2:11][CH:12]1[CH2:16][CH2:15][C:14]([CH3:18])([CH3:17])[CH2:13]1)[CH:21]=[C:22]2[CH2:23][CH2:24][NH:25][CH3:26]Participants
3
Procedure
The title compound is prepared by General Method 10 using 1-(4-chlorophenyl)-1-(2-(3,3-dimethylcyclopentyl)ethyl)hydrazine (Example 5) and 4,4-dimethoxy-N-methylbutan-1-amine.
Sources & evidence
- ORD record
- ord-402c59571e0c48d5b06d45c62b601f2e
- Source dataset
- uspto-grants-2016_02